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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1183341 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
: S4 g5 E8 T$ E( e* ]8 j$ i1 l8 R5 {NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
5 ]) E4 q8 c4 ], U+ Author Affiliations
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- @# ^. p/ l9 m. E1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
# x) H  U9 u' L. C* I! M1 L2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * g- ]9 @2 g& C6 P
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; l; Q$ T3 K, f" ?( l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ( Z7 J1 Y6 [7 ]1 p/ u
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan * a' ]  H& F, J$ H. V- W8 b. u  p
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 2 M2 A$ X# n- T, f! {& ^! c( a
7Kinki University School of Medicine, Osaka 589-8511, Japan
. J# P. |0 c! A$ }8Izumi Municipal Hospital, Osaka 594-0071, Japan ( F' W9 d, M: x+ h* c. o) e4 j
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan % ?  c# j0 G, K+ E  p8 y
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
6 G7 e5 S: e5 C0 j& I1 O* {7 t/ zAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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$ O. t& A  Y( ?- CAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato $ r3 l! d- }+ P8 I" P/ m

% F1 }5 u% Q1 z* y# v# x  RAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  , _  r2 ], G' j  _
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Published online on: Thursday, December 1, 2011
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( e  e0 i- B: M9 g0 N) R; c) x; nDoi: 10.3892/ol.2011.507 $ Z$ w( b- p3 |( J# C; y4 E
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Pages: 405-410
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Abstract:
. E) R! X$ e4 {S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population1 t' ]3 ?& ?7 R% n
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 w' q- z) A/ ]& ?
+ Author Affiliations
9 K, ]- n' m4 |6 J) i1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 4 V  x1 W, ]  c+ i  X" r% \9 I. m
2Department of Thoracic Surgery, Kyoto University, Kyoto
4 l! a9 I2 ?0 \' p$ D7 u3 B1 ?0 U- ]3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan . d$ u: j; }, ^5 k
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
- R9 U9 D: P3 C4 E5 b& h" Q& O4 eReceived September 3, 2010.
/ j( |- R/ A3 K( J- RRevision received November 11, 2010. ' S/ v  ?6 F5 H$ a$ b
Accepted November 17, 2010. 0 F& |; T; S; H. X8 t
Abstract
% W' k7 X) V- U3 {# U0 ABackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
5 i" ~% {2 y- C+ g8 O8 Z: ^Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
7 a; T( f; \, ~4 ?; NResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. 1 n' B0 z8 v! `7 p) A, y$ f
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 6 P& y$ {, L/ R" c0 X
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
5 b4 a: s; b2 l+ T& r# A, p& C) i今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
$ b5 L' s8 L1 f3 U' C& ^6 z6 y6 Chttp://clinicaltrials.gov/ct2/show/NCT01523587
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" \) B- Q( C$ t. r9 I& fBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC, i( _& y; N/ b; ^
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑   ?- z# k% h, C' ?' {  G
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。* k% |" b3 o2 S3 s! E
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
" W/ C! D* ]/ f7 E8 t5 a从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
4 `# M/ Z0 ?' @- Z3 G; L! P$ h  T' }至今为止,未出 ...

- G! }8 k( T6 |+ k0 W( Y没有副作用是第一追求,效果显著是第二追求。
; \' B9 e# x+ `3 E5 x不错。

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